Canonical Allele Identifier: CA1261033936

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601359G= , CM000664.2:g.73601359G=	GRCh38
NC_000002.11:g.73828486G= , CM000664.1:g.73828486G=	GRCh37
NC_000002.10:g.73681994G=	NCBI36
NG_011690.1:g.220607G= , LRG_741:g.220607G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11656G=	ENSP00000507671.1:p.Gly3886=
ENST00000682801.1:c.11167-826G=	ENSP00000507862.1:n.11167-826G=
ENST00000682859.1:c.11656G=	ENSP00000508222.1:p.Gly3886=
ENST00000683791.1:c.4742G=
ENST00000684460.1:c.8937G=
ENST00000684548.1:c.11656G=	ENSP00000507421.1:p.Gly3886=
ENST00000684590.1:c.6103G=	ENSP00000507376.1:p.Gly2035=
ENST00000684656.1:c.9121G=
ENST00000613296.6:c.12037G= MANE Select	ENSP00000482968.1:p.Gly4013=
ENST00000651057.1:c.2191G=	ENSP00000498504.1:p.Gly731=
ENST00000651434.1:c.3393G=
ENST00000651750.1:c.1260+478G=
ENST00000652487.1:c.3208G=
ENST00000464408.3:n.212G=
ENST00000484298.5:c.11911G=	ENSP00000478155.1:p.Gly3971=
ENST00000613296.4:c.12037G=	ENSP00000482968.1:p.Gly4013=
ENST00000620466.4:n.5840G=
NM_015120.4:c.12040G= , LRG_741t1:c.12040G=	NP_055935.4:p.Gly4014=
NM_001378454.1:c.12037G= MANE Select	NP_001365383.1:p.Gly4013=